EP0971940A1 - Diphosphines - Google Patents

Diphosphines

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Publication number
EP0971940A1
EP0971940A1 EP98921417A EP98921417A EP0971940A1 EP 0971940 A1 EP0971940 A1 EP 0971940A1 EP 98921417 A EP98921417 A EP 98921417A EP 98921417 A EP98921417 A EP 98921417A EP 0971940 A1 EP0971940 A1 EP 0971940A1
Authority
EP
European Patent Office
Prior art keywords
group
diphosphine
phospha
decyl
trioxatricyclo
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP98921417A
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German (de)
English (en)
Other versions
EP0971940B1 (fr
Inventor
Jacoba Catherina Lucia Johanna Suykerbuyk
Eit Drent
Paul Gerard Pringle
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Mitsubishi Chemical UK Ltd
Original Assignee
Shell Internationale Research Maatschappij BV
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Publication date
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Priority to EP98921417A priority Critical patent/EP0971940B1/fr
Publication of EP0971940A1 publication Critical patent/EP0971940A1/fr
Application granted granted Critical
Publication of EP0971940B1 publication Critical patent/EP0971940B1/fr
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Expired - Lifetime legal-status Critical Current

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2442—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/2461—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as ring members in the condensed ring system or in a further ring
    • B01J31/248—Bridged ring systems, e.g. 9-phosphabicyclononane
    • B01J31/2485—Tricyclic systems, e.g. phosphaadamantanes and hetero analogues
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
    • C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
    • C07C51/14—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on a carbon-to-carbon unsaturated bond in organic compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/36—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates
    • C07C67/38—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates by addition to an unsaturated carbon-to-carbon bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
    • C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
    • C07F9/65683—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a phosphine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
    • C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
    • C07F9/657163—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32—Addition reactions to C=C or C-C triple bonds
    • B01J2231/321—Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/822—Rhodium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/824—Palladium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/828—Platinum

Definitions

  • the invention relates to novel diphosphmes, novel carbonylation catalysts and a process for the carbonylation of unsaturated compounds by reaction thereof with carbon monoxide and a coreactant in the presence of the novel carbonylation catalysts.
  • Carbonylation reactions are known m the art. For instance, in EP-A-0, 495, 547 several examples are disclosed wherein olefms are converted into (thio) esters, acids, anhydrides, and amides, etc., depending on the nature of the coreactant. Other examples on the synthesis of aldehydes; ketones; carboxylic acids; esters; amides and other carboxylic acid derivatives; lactones; lactams and related N-heterocycles as well as background references can be found in "Carbonylation” by Messrs H M Colquhoun, D J Thompson and M V Twigg (Plenum press 1991) .
  • the rate of reaction is m the order of up to several hundreds moles product per mol catalyst (based on the metal) per hour. In case of internal unsaturation, the rate of reaction is even several orders lower. In other words, either relatively large amounts of catalyst are required or prolonged reaction times are involved.
  • the present inventors set out to provide a more active carbonylation catalyst. Surprisingly, carbonylation catalysts with high activity have been found that are obtainable by combining:
  • a metal cation selected from the groups 8, 9 or 10 of the Periodic Table of Elements and (ii) a diphosphine of the following formula R 1 >P-R 2 -PR 3 R 4 wherein R 2 represents a covalent bridging group, R! represents a bivalent radical that together with the phosphorus atom to which it is attached is an optionally substituted 2-phospha-tricyclo [3.3.1.1 ⁇ 3 , 7 ⁇ ] decyl group or a derivative thereof in which one or more of the carbon atoms are replaced by heteroatoms, and wherein R 3 and R 4 independently represent univalent radicals of up to 20 atoms or jointly form a bivalent radical of up to 20 atoms.
  • the diphosphines that may be used in the preparation of these carbonylation catalysts are believed to be novel too.
  • Tricyclo [3.3.1.1 ⁇ 3, 7 ⁇ ] decane is the systematic name for a compound more generally known as adamantane . Therefore, the optionally substituted 2-phospha-tricyclo- [3.3.1.1 ⁇ 3, 7 ⁇ decyl group will be referred to as "2-PA" group (as in 2-phosphadamantyl group) throughout the specification.
  • the 2-PA group is substituted on one or more of the 1, 3, 5 or 7 positions with a monovalent radical R ⁇ of up to 20 atoms.
  • R ⁇ include methyl, trifluoromethyl, ethoxy, phenyl, and 4- dodecylphenyl .
  • the 2-PA group is substituted on each of the 1, 3, 5 and 7 positions, suitably with identical radicals R ⁇ .
  • the 2-PA group has preferably additional heteroatoms other than the 2-phosphorus atom in its skeleton. Suitable heteroatoms are oxygen and sulphur atoms . Suitably, these heteroatoms are found in the 6, 9 and 10 positions .
  • the most preferred bivalent radical is the 2-phospha-
  • Each of the monovalent radicals R 3 and R 4 may independently be selected from (substituted) hydrocarbyl groups such as, for instance, methyl, phenyl, pyridyl, or o, o-di (t-butoxy) phenyl , and (substituted) heterohydro- carbyl groups such as, for instance, trimethylsilyl or alkoxy groups.
  • R 3 and R 4 may together form a bivalent radical, such as 1, 6-hexylene, 1,3 or 1,4- cyclooctylene, etc.
  • R 3 and R 4 together form a 2-PA group, most preferably a bivalent radical identical to R 1 .
  • the preferred ligands to be used in the carbonylation catalysts of the present invention are l,2-P,P'-di (2-phospha-l ,3,5, 7-tetramethyl-6, 9, 10-trioxatricyclo-
  • the ligand so defined can be prepared in a manner similar to the process for preparing the secondary phosphine 1,3,5, 7-tetramethyl-2 , 4 , 8-trioxa-6-phospha- adamantane disclosed in chapter 3 of "PRECIOUS METAL COMPLEXES OF SOME NOVEL FUNCTIONALISED SECONDARY AND TERTIARY PHOSPHINES" by Ms. Joanne H Downing (theses submitted to the University of Bristol on November 1992) . For instance, DPA3 is prepared by adding 2, 4-pentanedione to 1 , 3-diphosphinopropane .
  • Asymmetric ligands may be prepared using, for instance, a diphosphine having a tertiary phosphino group and a primary phosphino group. Alternatively, they may be prepared by coupling a secondary 2-phospha-tricyclo [3.3.1.1 ( 3, 7 ⁇ decane with another secondary monophosphine or by other processes known in the art. Substituted ligands can, for example, be made using substituted 2 , 4-pentanediones such as perfluoro-2, 4-pentanedione or 1 , 1, 1, 5, 5 , 5-hexfluoro-2 , 4- pentanedione in the reaction with the phosphine .
  • group 8, 9 and 10 metal cations are cations of Fe, Ru, Os; Co, Rh, Ir and Ni, Pd, and Pt, respectively. These cations, as is illustrated in “Carbonylation”, may each be used in the various carbonylation reactions.
  • Group 9 metal cations, and Group 10 metal cations (referred to in the older literature as the platinum group metal cations) have been found to provide particularly good results when used in the novel catalyst of the present invention.
  • Suitable sources for the metal cations may be found in "Carbonylation" and will form no problem to the person skilled in the art.
  • the preparation of the catalyst system (actually a precursor, the active species formed in-situ may be slightly different from that of the precursor here disclosed) follows the general recipe disclosed in the thesis by Ms J H Downing.
  • the catalyst systems may be used in the various carbonylation reactions described in EP-A-0, 495 , 547 and in "Carbonylation". They particularly excel in respect of the reaction rate when applied in the additive carbonylation of unsaturated compounds, notably of ethylenically unsaturated compounds.
  • the latter reaction here shown for an alpha-olefin, proceeds according to the following reaction:
  • the catalyst systems may be used in any order.
  • anions may be used as counter-ion to the metal cation.
  • examples thereof include anions that are the conjugated base of acids having a pKa (measured at
  • the anions derived from these acids do not or only weakly co-ordinate with the metal cation, by which is meant that little or no covalent interaction occurs between the anion and the cation. Catalysts based on these anions exhibit a good activity.
  • Suitable anions include anions derived from Bronsted acids, such as from phosphoric acid and sulphuric acid, and in particular from sulphonic acids and (halogenated) carboxylic acids, such as trifluoroacetic acid, 2,6-di- chlorobenzoic acid, and 2 , 6-bis ( trifluoromethyl) benzoic acid or trifluoroacetic acid, etc.
  • Anions derived from sulphonic acids are particularly preferred, for example methanesulphonic acid, trifluoromethanesulphonic acid, tert-butanesulphonic acid, p-toluenesulphonic acid and
  • complex anions are suitable, such as the anions generated by a combination of a Lewis acid such as BF3, B(C 6 F 5 ) 3 , A1C1 3 , SnF 2 , Sn(CF 3 S0 3 ) 2 , SnCl 2 or GeCl 2 , with a protic acid, preferably having a pKa of less than 5, such as a sulphonic acid, e.g. CF3SO3H or CH3SO3H or a hydrohalogenic acid such as HF or HC1, or a combination of a Lewis acid with an alcohol.
  • a Lewis acid such as BF3, B(C 6 F 5 ) 3 , A1C1 3 , SnF 2 , Sn(CF 3 S0 3 ) 2 , SnCl 2 or GeCl 2
  • a protic acid preferably having a pKa of less than 5, such as a sulphonic acid, e.g. CF3SO3H or CH3SO3
  • the carbonylation reaction is conveniently carried out at moderate temperatures. Accordingly, the process is suitably carried out at a temperature in the range of 30 to 200 °C, preferred temperatures being in the range of 50 to 180 °C.
  • the reaction pressures may also vary widely. For instance, the reaction can be carried out with pressures in the range of 1 to 200 bar gauge, pres- sures in the range of 5 to 60 barg being preferred.
  • Carbon monoxide is preferably supplied in molar excess over the unsaturated compound and the coreactant "YH" .
  • the unsaturated compound and the coreactant are suitably supplied in a molar ratio within the range of 10:1 to 1:10, preferably within the range of 5:1 to 1:5, more preferably within the range of 2:1 to 1:2.
  • the quantity in which the catalyst system is used is not critical and may vary within wide limits . Usually amounts in the range of 10 " ⁇ to 10 ⁇ 1, preferably in the range of 10 "" ⁇ to 10 ⁇ 2 mole atom of metal per mole of unsaturated compound are used.
  • the amount of ligand is generally applied in some excess of the amount of the metal cation, expressed as moles of ligand per mole atom of the cation.
  • the amount of ligand is selected such that per mole atom of the cation 0.5 to 10 moles of ligand are present.
  • the active species is believed to be based on an equimolar amount of bidentate ligand per mole cation.
  • the molar amount of bidentate ligand per mole of cation is preferably in the range of 1 to 3, more preferably in the range of 1 to 2. In the presence of oxygen, slightly higher amounts may be beneficial.
  • the amount of the anion source may range from 0.5 to 15, preferably from 1 to 8 moles per mole of cation .
  • the starting materi- als and the formed carbonylation products may act as reaction diluent.
  • the carbonylation reaction may be carried out in the additional presence of a solvent.
  • saturated hydrocarbons such as, e.g., paraffins and isoalkanes are recommended and furthermore ethers such as 2 , 5, 8-trioxanonane (diglyme), diethylether and anisole; sulphones such as sulpholane, and aromatic hydrocarbons such as toluene.
  • the unsaturated compound may have one or more unsatu- rated bonds and is preferably an olefin having from 2 to 30 carbon atoms per molecule.
  • the unsaturated bond(s) may be internal or terminal, the catalyst being particularly advantageous in the conversion of internal olefins.
  • Particularly preferred are olefins having from 2 to 22 carbon atoms per molecule, such as ethene, propene, 1- or 2-butene, 1- or internal hexene, 1 or internal octene, diisobutylene, triisobutylene, tripropylene, internal de- cene, internal C_4 olefins, and internal C ⁇ 5 ⁇ C]_g olefins.
  • one or more hydrogen atoms may have been substituted by other atoms, such as halogen atoms or by groups of atoms, such as hydroxyl groups, cyano groups, such as methoxy or ethoxy groups, or amino groups such as dimethyl- and diethyl-amino groups .
  • Another preferred category of unsaturated compounds consists of unsaturated esters of carboxylic acids and esters of unsaturated carboxylic acids.
  • the starting material may be a vinyl ester of a carboxylic acid such as acetic acid or propanoic acid, or it may be an alkyl ester of an unsaturated acid, such as the methyl or ethyl ester of acrylic acid or methacrylic acid.
  • a further preferred category of unsaturated compounds consists of cycloalkadienes , which will ordinar- ily refuse carbonylation.
  • the starting material may be dicyclopentadiene or norbornadiene, to give diesters, diamides or diacids, etc., which may find use as monomer in polymerization reactions.
  • Suitable coreactants in the additive carbonylation process of the invention include compounds comprising a nucleophilic moiety and a mobile hydrogen atom.
  • Preferred nucleophilic compounds include: molecular hydrogen, water and alcohols, e.g., monohydric alcohols, such as methanol, ethanol, isopropanol and 1-butanol, and polyhydric alcohols, such as ethyleneglycol, 1,4-butane- diol and glycerol; thiols; primary or secondary (poly-) amines or amides, such as diethylamine, N,N-dimethyl ethylenediamine; aromatic alcohols and carboxylic acids, for example acetic acid, pivalic acid and propanoic acid.
  • monohydric alcohols such as methanol, ethanol, isopropanol and 1-butanol
  • polyhydric alcohols such as ethyleneglycol, 1,4-butane- diol and glycerol
  • thiols primary or secondary (poly-) amines or amides, such as diethylamine, N,N-dimethyl ethylene
  • 1-Butanol, methanol and 1 , 4-butanediol are especially preferred.
  • the use of these compounds as coreactants enables the production of valuable carbonylation products, such as methyl propanoate, butyl propanoate and 1 , 4-diacyloxy butanes.
  • These compounds are of commercial interest and may be used as solvents and in flavouring compositions and perfumes.
  • Another preferred class of coreactants is composed of alkylphenols, wherein one or more alkyl groups of up to 30, typically 6 to 22 carbon atoms are attached to the phenol molecule. Additive carbonylation with these coreactants produces alkylphenyl esters that may find use as synthetic lubricants in industrial application, but in particular in automotive engines.
  • DPA3 l,3-P,P'-di (2-phospha-l,3,5,7-tetramethyl-6, 9,10- trioxatricyclo[3.3.1.1(3.7 ⁇ decyl) propane
  • MSA methanesulphonic acid
  • Example 1 (Synthesis of the ligands) 4.63 Mmol diphosphinopropane was added to a solution of 27.8 mmol 2 , 4-pentanedione in 20 ml 5M HCl. After 1 hr stirring a white solid began to precipitate. The reaction mixture was stirred for a further 24 hrs, and then the volatile components were removed to leave a white, air- stable solid product.
  • the autoclave was charged with 50 ml of methanol, 0.1 mmol of palladium ( II ) acetate, 0.15 mmol of DPA3, and 0.2 mmol of MSA. After being flushed, the autoclave was pressurised with carbon monoxide and ethene to a partial pressure of 30 bar and 20 bar respectively. Next, the reactor was sealed. The contents of the autoclave were heated to a temperature of 90 °C and maintained at that temperature for 0.25 hours. After cooling, a sample was taken from the contents of the autoclave and analysed by Gas Liquid Chromatography .
  • Example 2 was repeated, however using 10 ml water and 40 ml of diglyme as reactant/solvent and a process temperature of 110 °C. The autoclave was cooled after
  • Example 2 was repeated, however using 30 ml propene as olefin and a process temperature of 100 °C. Propene was fully converted with 78% selectivity into methyl butanoate and 22% selectivity into methyl 2-methylpropanoate at an average rate of 5000 mol/mol. hr.
  • Example 5
  • Example 2 was repeated, however using 20 ml of an alpha-C ⁇ 4 olefin feed. The autoclave was cooled after
  • Example 2 was repeated, however using 20 ml of an internal-C_4 olefin feed, at a process temperature of 115 °C, and at a carbon monoxide pressure of 10 bar. The autoclave was cooled after 5 hours.
  • Example 6 The internal olefins were converted for 93% with 78% selectivity into linear methyl esters at an average rate of 120 mol/mol.hr. Comparative Example A Example 6 was repeated, however using l,3-bis(di- tert-butylphosphino) propane as ligand, and at a carbon monoxide pressure of 10 and 30 bar, respectively. The autoclave was cooled after 10 hours.
  • Example 2 was repeated, however using 10 ml methyl 3-pentenoate as unsaturated compound, at a process temperature of 115 °C and at a carbon monoxide pressure of 15 bar. The autoclave was cooled after 6 hours.
  • Example 2 was repeated, however using 0.1 mmol of platinum(II) acetylacetonate, 0.12 mmol of DPA3, and 0.25 mmol of MSA. Besides, the contents of the autoclave were heated to 125 °C . The autoclave was cooled after 3 hours.
  • Example 8 was repeated, however using l,3-bis(di- tert-butylphosphino) propane as ligand.
  • Methyl propionate was now formed at an average rate of only 10 mol/mol.hr.
  • the autoclave was charged with 50 ml diglyme, 0.1 mmol rhodium dicarbonyl acetylacetonate, and 0.12 mmol of DPA3. After being flushed, the autoclave was charged with 15 ml propene and pressurised with carbon monoxide and hydrogen to a partial pressure of 25 bar and 25 bar each. Next, the reactor was sealed. The contents of the autoclave were heated to a temperature of 80 °C and maintained at that temperature for 0.25 hours. After cooling, a sample was taken from the contents of the autoclave and analysed by GLC .
  • Example 9 was repeated, however using 0.1 mmol of DPA2.
  • Example 9 was repeated, however using 10 ml of vinyl acetate instead of propene, 50 ml of toluene instead of diglyme and 0.2 mmol of DPA3. Besides, the autoclave was heated to a temperature of 115 °C .
  • Vinyl acetate was fully converted into a mixture of 1-formylethyl acetate and 2-formylethyl acetate (mole ratio 10:1) at an average rate of 5000 mol/mol.hr.

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Abstract

L'invention se rapporte à une diphosphine de la formule suivante: R?1>P-R2-PR3R4¿ dans laquelle R2 représente un groupe de pontage covalent; R1 représente un radical bivalent qui, avec l'atome de phosphore auquel il est fixé, représente un groupe 2-phosphatricyclo [3.3.1.1.<3,7>]décyle éventuellement substitué, ou un dérivé de ce groupe, dans lequel un ou plusieurs des atomes de carbone sont remplacés par des hétéroatomes (groupe '2-PA'); R3 et R4 représentent indépendamment des radicaux univalents pouvant contenir jusqu'à 20 atomes ou qui forment ensemble un radical bivalent pouvant contenir jsuqu'à 20 atomes. L'invention concerne en outre des catalyseurs de carbonylation que l'on peut obtenir par combinaison (i) d'un cation métallique sélectionné à partir des groupes (8, 9 ou 10) de la classification périodique des éléments et (ii) de la nouvelle diphosphine. L'invention concerne enfin un procédé permettant de réaliser la carbonylation de composés non saturés en présence du catalyseur de carbonylation.
EP98921417A 1997-03-26 1998-03-25 Diphosphines Expired - Lifetime EP0971940B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP98921417A EP0971940B1 (fr) 1997-03-26 1998-03-25 Diphosphines

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
EP97302079 1997-03-26
EP97302079 1997-03-26
EP97302958 1997-04-30
EP97302958 1997-04-30
PCT/EP1998/001916 WO1998042717A1 (fr) 1997-03-26 1998-03-25 Diphosphines
EP98921417A EP0971940B1 (fr) 1997-03-26 1998-03-25 Diphosphines

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EP0971940A1 true EP0971940A1 (fr) 2000-01-19
EP0971940B1 EP0971940B1 (fr) 2002-06-05

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JP4201846B2 (ja) 2008-12-24
US6156934A (en) 2000-12-05
DE69805789D1 (de) 2002-07-11
WO1998042717A1 (fr) 1998-10-01
AU7428498A (en) 1998-10-20
DE69805789T2 (de) 2003-01-02
JP2001520659A (ja) 2001-10-30
EP0971940B1 (fr) 2002-06-05
TW528759B (en) 2003-04-21

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